Deregulation of miR-93 and miR-143 in human esophageal cancer
Esophageal squamous cell carcinoma (ESCC) is the second and third most common malignancy in Iranian males and females, respectively. Treatment of ESCC is largely ineffective due to lack of detection at early stages of the disease. In recent years, miRNA, a small RNA molecule, has drawn much attentio...
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Veröffentlicht in: | Tumor biology 2016-03, Vol.37 (3), p.3097-3103 |
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description | Esophageal squamous cell carcinoma (ESCC) is the second and third most common malignancy in Iranian males and females, respectively. Treatment of ESCC is largely ineffective due to lack of detection at early stages of the disease. In recent years, miRNA, a small RNA molecule, has drawn much attention to researchers as a potential biomarker for esophageal cancer.
miR-93
and
miR-143
are two miRNA molecules reported to be frequently deregulated in various cancers, including prostate, stomach, cervix, and etc. The purpose of this study was to investigate the expression levels of these miRNAs and evaluate their diagnostic and therapeutic potential in esophageal squamous cell carcinoma. In this study, total RNA was extracted from 30 tumor tissues and 30 nontumor tissues of esophageal tumor margins, using RNX-plus solution. After validating the quality and quantity of total RNA, cDNAs of interest were synthesized using microRNA-specific cDNA Synthesis Kit. The expression level of
miR-93
and
miR-143
was evaluated using quantitative real-time PCR with miRNA-specific primers. Finally, the obtained data was analyzed by SPSS ver.20 software and paired
t
test was performed to observe the significance of difference between groups. The expression level of
miR-93
was significantly increased and of
miR-143
was significantly decreased in most of the examined tumor tissues, compared to nontumor tissues. Also, our findings did not detect correlation between mir-93 and mir-143 expressions in regard to stage and grade of the samples. These findings suggest that the deregulation of these miRNAs may play an important role in esophageal squamous cell carcinoma. Both
miR-93
and
miR-143
might be used as potential biomarkers in esophageal squamous cell carcinoma. However, more studies with large population of samples are necessary. |
doi_str_mv | 10.1007/s13277-015-3987-9 |
format | Article |
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miR-93
and
miR-143
are two miRNA molecules reported to be frequently deregulated in various cancers, including prostate, stomach, cervix, and etc. The purpose of this study was to investigate the expression levels of these miRNAs and evaluate their diagnostic and therapeutic potential in esophageal squamous cell carcinoma. In this study, total RNA was extracted from 30 tumor tissues and 30 nontumor tissues of esophageal tumor margins, using RNX-plus solution. After validating the quality and quantity of total RNA, cDNAs of interest were synthesized using microRNA-specific cDNA Synthesis Kit. The expression level of
miR-93
and
miR-143
was evaluated using quantitative real-time PCR with miRNA-specific primers. Finally, the obtained data was analyzed by SPSS ver.20 software and paired
t
test was performed to observe the significance of difference between groups. The expression level of
miR-93
was significantly increased and of
miR-143
was significantly decreased in most of the examined tumor tissues, compared to nontumor tissues. Also, our findings did not detect correlation between mir-93 and mir-143 expressions in regard to stage and grade of the samples. These findings suggest that the deregulation of these miRNAs may play an important role in esophageal squamous cell carcinoma. Both
miR-93
and
miR-143
might be used as potential biomarkers in esophageal squamous cell carcinoma. However, more studies with large population of samples are necessary.</description><identifier>ISSN: 1010-4283</identifier><identifier>EISSN: 1423-0380</identifier><identifier>DOI: 10.1007/s13277-015-3987-9</identifier><identifier>PMID: 26427659</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Aged ; Biomarkers ; Biomedical and Life Sciences ; Biomedicine ; Cancer Research ; Carcinoma, Squamous Cell - etiology ; Carcinoma, Squamous Cell - genetics ; Esophageal cancer ; Esophageal Neoplasms - etiology ; Esophageal Neoplasms - genetics ; Esophageal Squamous Cell Carcinoma ; Female ; Gene Expression Regulation, Neoplastic ; Humans ; Male ; MicroRNAs ; MicroRNAs - physiology ; Middle Aged ; Original Article ; Studies</subject><ispartof>Tumor biology, 2016-03, Vol.37 (3), p.3097-3103</ispartof><rights>International Society of Oncology and BioMarkers (ISOBM) 2015</rights><rights>International Society of Oncology and BioMarkers (ISOBM) 2016</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-82a08111751823af573ca5a02738cc0b547420767f6e35b2437e943b42f8ce293</citedby><cites>FETCH-LOGICAL-c438t-82a08111751823af573ca5a02738cc0b547420767f6e35b2437e943b42f8ce293</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s13277-015-3987-9$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s13277-015-3987-9$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26427659$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ansari, Mohammad Hossein</creatorcontrib><creatorcontrib>Irani, Shiva</creatorcontrib><creatorcontrib>Edalat, Houri</creatorcontrib><creatorcontrib>Amin, Ruhul</creatorcontrib><creatorcontrib>Mohammadi Roushandeh, Amaneh</creatorcontrib><title>Deregulation of miR-93 and miR-143 in human esophageal cancer</title><title>Tumor biology</title><addtitle>Tumor Biol</addtitle><addtitle>Tumour Biol</addtitle><description>Esophageal squamous cell carcinoma (ESCC) is the second and third most common malignancy in Iranian males and females, respectively. Treatment of ESCC is largely ineffective due to lack of detection at early stages of the disease. In recent years, miRNA, a small RNA molecule, has drawn much attention to researchers as a potential biomarker for esophageal cancer.
miR-93
and
miR-143
are two miRNA molecules reported to be frequently deregulated in various cancers, including prostate, stomach, cervix, and etc. The purpose of this study was to investigate the expression levels of these miRNAs and evaluate their diagnostic and therapeutic potential in esophageal squamous cell carcinoma. In this study, total RNA was extracted from 30 tumor tissues and 30 nontumor tissues of esophageal tumor margins, using RNX-plus solution. After validating the quality and quantity of total RNA, cDNAs of interest were synthesized using microRNA-specific cDNA Synthesis Kit. The expression level of
miR-93
and
miR-143
was evaluated using quantitative real-time PCR with miRNA-specific primers. Finally, the obtained data was analyzed by SPSS ver.20 software and paired
t
test was performed to observe the significance of difference between groups. The expression level of
miR-93
was significantly increased and of
miR-143
was significantly decreased in most of the examined tumor tissues, compared to nontumor tissues. Also, our findings did not detect correlation between mir-93 and mir-143 expressions in regard to stage and grade of the samples. These findings suggest that the deregulation of these miRNAs may play an important role in esophageal squamous cell carcinoma. Both
miR-93
and
miR-143
might be used as potential biomarkers in esophageal squamous cell carcinoma. However, more studies with large population of samples are necessary.</description><subject>Aged</subject><subject>Biomarkers</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cancer Research</subject><subject>Carcinoma, Squamous Cell - etiology</subject><subject>Carcinoma, Squamous Cell - genetics</subject><subject>Esophageal cancer</subject><subject>Esophageal Neoplasms - etiology</subject><subject>Esophageal Neoplasms - genetics</subject><subject>Esophageal Squamous Cell Carcinoma</subject><subject>Female</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Humans</subject><subject>Male</subject><subject>MicroRNAs</subject><subject>MicroRNAs - physiology</subject><subject>Middle Aged</subject><subject>Original Article</subject><subject>Studies</subject><issn>1010-4283</issn><issn>1423-0380</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kE1LAzEQhoMotlZ_gBdZ8OIlmmSSTXLwIPUTCoLoOaRptt2yHzXpHvz3Zt0qIniagXnmneFB6JSSS0qIvIoUmJSYUIFBK4n1HhpTzgATUGQ_9YQSzJmCETqKcU0SqHV-iEYs50zmQo_R9a0PftlVdlu2TdYWWV2-YA2ZbRZfLeWQlU226mrbZD62m5VdeltlzjbOh2N0UNgq-pNdnaC3-7vX6SOePT88TW9m2HFQW6yYJYpSKgVVDGwhJDgrLGESlHNkLrjkjMhcFrkHMWccpNcc5pwVynmmYYIuhtxNaN87H7emLqPzVWUb33bRUKlSRFpRCT3_g67bLjTpu54CDVzwnqID5UIbY_CF2YSytuHDUGJ6t2Zwa5Iy07s1_RNnu-RuXvvFz8a3zASwAYhp1Cx9-HX639RPzJ5_kA</recordid><startdate>20160301</startdate><enddate>20160301</enddate><creator>Ansari, Mohammad Hossein</creator><creator>Irani, Shiva</creator><creator>Edalat, Houri</creator><creator>Amin, Ruhul</creator><creator>Mohammadi Roushandeh, Amaneh</creator><general>Springer Netherlands</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7TO</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>20160301</creationdate><title>Deregulation of miR-93 and miR-143 in human esophageal cancer</title><author>Ansari, Mohammad Hossein ; Irani, Shiva ; Edalat, Houri ; Amin, Ruhul ; Mohammadi Roushandeh, Amaneh</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c438t-82a08111751823af573ca5a02738cc0b547420767f6e35b2437e943b42f8ce293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Aged</topic><topic>Biomarkers</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cancer Research</topic><topic>Carcinoma, Squamous Cell - etiology</topic><topic>Carcinoma, Squamous Cell - genetics</topic><topic>Esophageal cancer</topic><topic>Esophageal Neoplasms - etiology</topic><topic>Esophageal Neoplasms - genetics</topic><topic>Esophageal Squamous Cell Carcinoma</topic><topic>Female</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Humans</topic><topic>Male</topic><topic>MicroRNAs</topic><topic>MicroRNAs - physiology</topic><topic>Middle Aged</topic><topic>Original Article</topic><topic>Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ansari, Mohammad Hossein</creatorcontrib><creatorcontrib>Irani, Shiva</creatorcontrib><creatorcontrib>Edalat, Houri</creatorcontrib><creatorcontrib>Amin, Ruhul</creatorcontrib><creatorcontrib>Mohammadi Roushandeh, Amaneh</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Tumor biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ansari, Mohammad Hossein</au><au>Irani, Shiva</au><au>Edalat, Houri</au><au>Amin, Ruhul</au><au>Mohammadi Roushandeh, Amaneh</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Deregulation of miR-93 and miR-143 in human esophageal cancer</atitle><jtitle>Tumor biology</jtitle><stitle>Tumor Biol</stitle><addtitle>Tumour Biol</addtitle><date>2016-03-01</date><risdate>2016</risdate><volume>37</volume><issue>3</issue><spage>3097</spage><epage>3103</epage><pages>3097-3103</pages><issn>1010-4283</issn><eissn>1423-0380</eissn><abstract>Esophageal squamous cell carcinoma (ESCC) is the second and third most common malignancy in Iranian males and females, respectively. Treatment of ESCC is largely ineffective due to lack of detection at early stages of the disease. In recent years, miRNA, a small RNA molecule, has drawn much attention to researchers as a potential biomarker for esophageal cancer.
miR-93
and
miR-143
are two miRNA molecules reported to be frequently deregulated in various cancers, including prostate, stomach, cervix, and etc. The purpose of this study was to investigate the expression levels of these miRNAs and evaluate their diagnostic and therapeutic potential in esophageal squamous cell carcinoma. In this study, total RNA was extracted from 30 tumor tissues and 30 nontumor tissues of esophageal tumor margins, using RNX-plus solution. After validating the quality and quantity of total RNA, cDNAs of interest were synthesized using microRNA-specific cDNA Synthesis Kit. The expression level of
miR-93
and
miR-143
was evaluated using quantitative real-time PCR with miRNA-specific primers. Finally, the obtained data was analyzed by SPSS ver.20 software and paired
t
test was performed to observe the significance of difference between groups. The expression level of
miR-93
was significantly increased and of
miR-143
was significantly decreased in most of the examined tumor tissues, compared to nontumor tissues. Also, our findings did not detect correlation between mir-93 and mir-143 expressions in regard to stage and grade of the samples. These findings suggest that the deregulation of these miRNAs may play an important role in esophageal squamous cell carcinoma. Both
miR-93
and
miR-143
might be used as potential biomarkers in esophageal squamous cell carcinoma. However, more studies with large population of samples are necessary.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>26427659</pmid><doi>10.1007/s13277-015-3987-9</doi><tpages>7</tpages></addata></record> |
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subjects | Aged Biomarkers Biomedical and Life Sciences Biomedicine Cancer Research Carcinoma, Squamous Cell - etiology Carcinoma, Squamous Cell - genetics Esophageal cancer Esophageal Neoplasms - etiology Esophageal Neoplasms - genetics Esophageal Squamous Cell Carcinoma Female Gene Expression Regulation, Neoplastic Humans Male MicroRNAs MicroRNAs - physiology Middle Aged Original Article Studies |
title | Deregulation of miR-93 and miR-143 in human esophageal cancer |
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